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dc.contributor.authorHerrero-Brocal, Marta-
dc.contributor.authorSamper Perez, Raquel-
dc.contributor.authorRiquelme, Jorge-
dc.contributor.authorPineda, Javier-
dc.contributor.authorBORDES SISCAR, PASCUAL-
dc.contributor.authorTorres Mezcua, Fernando José-
dc.contributor.authorValencia, José-
dc.contributor.authorTorres-Saura, Francisco-
dc.contributor.authorGonzález Manso, María-
dc.contributor.authorAjo Ferrer, Raquel-
dc.contributor.authorArenas, Juan-
dc.contributor.authorFeliu, Eloísa-
dc.contributor.authorMartínez, Juan Gabriel-
dc.contributor.authorRuiz-Nodar, Juan-
dc.contributor.otherDepartamentos de la UMH::Patología y Cirugíaes_ES
dc.date.accessioned2026-01-16T16:06:17Z-
dc.date.available2026-01-16T16:06:17Z-
dc.date.created2024-10-
dc.identifier.citationEuropean Heart Journal - Digital Health, 6(1), 73-81 - November 2024es_ES
dc.identifier.issn2634-3916-
dc.identifier.urihttps://hdl.handle.net/11000/38911-
dc.description.abstractAims: Evidence regarding the safety of early discharge following transcatheter aortic valve implantation (TAVI) is limited. The aim of this study was to evaluate the safety of very early (<24) and early discharge (24-48 h) as compared to standard discharge (>48 h), supported by the implementation of a voice-based virtual assistant using artificial intelligence (AI) and natural language processing. Methods and results: Single-arm prospective observational study that included consecutive patients who underwent TAVI in a tertiary hospital in 2023 and were discharged under an AI follow-up programme. Primary endpoint was a composite of death, pacemaker implantation, readmission for heart failure, stroke, acute myocardial infarction, major vascular complications, or major bleeding, at 30-day follow-up. A total of 274 patients were included. 110 (40.1%) patients were discharged very early (<24 h), 90 (32.9%) early (24-48 h), and 74 (27.0%) were discharged after 48 h. At 30-day follow-up, no significant differences were found among patients discharged very early, early, and those discharged after 48 h for the primary endpoint (very early 9.1% vs. early 11.1% vs. standard 9.5%; P = 0.88). The AI platform detected complications that could be effectively addressed. The implementation of this follow-up system was simple and satisfactory for TAVI patients. Conclusion: Early and very early discharge in patients undergoing TAVI, supported by close follow-up using AI, were shown to be safe. Patients with early and very early discharge had similar 30-day event rates compared to those with longer hospital stays. The AI system contributed to the early detection and resolution of complications.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent9es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectTranscatheter aortic valve implantation (TAVI)es_ES
dc.subjectEarly dischargees_ES
dc.subjectArtificial intelligence (AI)es_ES
dc.subjectTelemedicinees_ES
dc.subjectPost-discharge monitoringes_ES
dc.subjectComplication detectiones_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes_ES
dc.titleEarly discharge programme after transcatheter aortic valve implantation based on close follow-up supported by telemonitoring using artificial intelligence: the TeleTAVI studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.1093/ehjdh/ztae089es_ES
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Artículos Patología y Cirugía


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